Canonical Allele Identifier: PA915965481
Gene: GP1BB HGNC NCBI

Linked Data

ClinVar Variation Id: 627320
ClinVar RCV Id: RCV000852142 RCV001003916 RCV002222630 RCV003324792
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000398.1:p.Leu16Pro
CA410676273
NM_000407.5:c.47T>C